Abstract

The response to neoadjuvant chemoradiation (nCRT) is a critical step in the management of locally advanced rectal cancer (LARC) patients. Only a minority of LARC patients responds completely to neoadjuvant treatments, thus avoiding invasive radical surgical resection. Moreover, toxic side effects can adversely affect patients’ survival. The difficulty in separating in advances responder from non-responder patients affected by LARC highlights the need for valid biomarkers that guide clinical decision-making. In this context, microRNAs (miRNAs) seem to be promising candidates for predicting LARC prognosis and/or therapy response, particularly due to their stability, facile detection, and disease-specific expression in human tissues, blood, serum, or urine. Although a considerable number of studies involving potential miRNA predictors to nCRT have been conducted over the years, to date, the identification of the perfect miRNA signatures or single miRNA, as well as their use in the clinical practice, is still representing a challenge for the management of LARC patients. In this review, we will first introduce LARC and its difficult management. Then, we will trace the scientific history and the key obstacles for the identification of specific miRNAs that predict responsiveness to nCRT. There is a high potential to identify non-invasive biomarkers that circulate in the human bloodstream and that might indicate the LARC patients who benefit from the watch-and-wait approach. For this, we will critically evaluate recent advances dealing with cell-free nucleic acids including miRNAs and circulating tumor cells as prognostic or predictive biomarkers.

Highlights

  • Rectal cancer (RC) is one among the top four most deadly neoplasms worldwide [1]

  • This study revealed that thymidylate synthase (TYMS) messenger RNA transcripts (mRNAs) and/or TYMS/RAD23 homolog B (RAD23B) protein expression in circulating tumor cells (CTCs) have the potential to predict non-response to neoadjuvant chemoradiation (nCRT) and avoid unnecessary radical surgery for locally advanced rectal cancer (LARC) patients with pathological response (pCR) [114]

  • The assessment of the variation of levels of single or signatures of miRNAs in tumor specimens or, even better circulating miRNAs and/or tumor cells in body fluids, could improve the stratification of LARC patients according to the nCRT response, facilitating the clinical decision-making

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Summary

Introduction

Rectal cancer (RC) is one among the top four most deadly neoplasms worldwide [1]. In the last three decades, high-income countries experienced a reduction in the incidence of RC, as well as a decrease of its mortality, maybe due to both diagnostic/therapeutic improvements and secondary prevention. A retrospective analysis showed that unsuccessful multidisciplinary discussion was one of the predictive factors for positive resection margins, as well as the absence of radiotherapy [4]. We will enumerate diagnostic and treatment challenges encountered when dealing with advanced rectal cancer. Due to the increasing impact of circulating biomarkers in cancer care, we will provide an overview of the involvement of circulating miRNAs, as well as single nucleotide polymorphisms (SNPs) associated with miRNAs (miR-SNPs) in the prediction of response to nCRT treatment. We will inspect the recent advances on the potential predictive role of other circulating tumor markers in LARC, with a particular focus on the cell-free (cf) nucleic acids and circulating tumor cells (CTCs)

Diagnostic Work-Up
The Concept of Tumor Regression Rate
Assessing Clinical Response
The Watch and Wait Approach
Circulating Biomarkers to Predict Response to nCRT in LARC
Exosomal microRNAs in LARC
Circulating Derived Tumor-Proteins in LARC
Findings
Conclusions
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